Since most patients with cystic fibrosis (CF) die from respiratory failure, lung transplantation remains for many of them the ultimate treatment. The decision to put a patient on the transplantation waiting list is based on a list of criteria from international guidelines. We aimed to determine if a survival score could help determine when a CF patient has to be referred to a transplantation program. We applied this score to a small number of consecutive patients from our adult CF clinic, but found that it was of limited value for individual decision. Awareness of international guidelines and clinical judgement are essential to refer CF patients at proper time for lung transplantation
AbstractBackgroundCystic fibrosis (CF) remains a lethal condition where a palliative approach is oft...
Lung transplantation represents the only therapeutic option for patients affected by end-stage cysti...
AbstractObjective: Lung transplantation is a viable option for patients with cystic fibrosis. The cu...
Abstract Background Cystic Fibrosis (CF) Centers are involved in the decisions regarding the eligibi...
Cystic fibrosis is a common indication for lung transplantation. Under the current organ allocation ...
Lung transplantation is a complex, high-risk, potentially life-saving therapy for the end-stage lung...
There are no European recommendations on issues specifically related to lung transplantation (LTX) i...
International audienceStudies of large CF populations using registry data are important to identify ...
Cystic Fibrosis is unfortunately an incurable inherited disorder. Despite real progress in research,...
Objectives. (1) Identify the decisional needs of cystic fibrosis patients considering referral for b...
There are no European recommendations on issues specifically related to lung transplantation (LTX) i...
International audienceBackground: Therapeutic progress in patients with cystic fibrosis (CF) has res...
Lung transplantation should be considered in cystic fibrosis patients with end-stage lung disease. T...
BACKGROUND: Cystic fibrosis (CF) is congenital multisystem disorder, that leads to gradual deteriora...
Survival in patients with cystic fibrosis (CF) has improved dramatically over the past 30 to 40 year...
AbstractBackgroundCystic fibrosis (CF) remains a lethal condition where a palliative approach is oft...
Lung transplantation represents the only therapeutic option for patients affected by end-stage cysti...
AbstractObjective: Lung transplantation is a viable option for patients with cystic fibrosis. The cu...
Abstract Background Cystic Fibrosis (CF) Centers are involved in the decisions regarding the eligibi...
Cystic fibrosis is a common indication for lung transplantation. Under the current organ allocation ...
Lung transplantation is a complex, high-risk, potentially life-saving therapy for the end-stage lung...
There are no European recommendations on issues specifically related to lung transplantation (LTX) i...
International audienceStudies of large CF populations using registry data are important to identify ...
Cystic Fibrosis is unfortunately an incurable inherited disorder. Despite real progress in research,...
Objectives. (1) Identify the decisional needs of cystic fibrosis patients considering referral for b...
There are no European recommendations on issues specifically related to lung transplantation (LTX) i...
International audienceBackground: Therapeutic progress in patients with cystic fibrosis (CF) has res...
Lung transplantation should be considered in cystic fibrosis patients with end-stage lung disease. T...
BACKGROUND: Cystic fibrosis (CF) is congenital multisystem disorder, that leads to gradual deteriora...
Survival in patients with cystic fibrosis (CF) has improved dramatically over the past 30 to 40 year...
AbstractBackgroundCystic fibrosis (CF) remains a lethal condition where a palliative approach is oft...
Lung transplantation represents the only therapeutic option for patients affected by end-stage cysti...
AbstractObjective: Lung transplantation is a viable option for patients with cystic fibrosis. The cu...